View genomic variant #0000003416

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.133333869C>T
Published as -
GERP 4.880
Segregation -
DB-ID ASS1_000011
MSCV MSCV_0003416
dbSNP ID rs121908644
Frequency -
Sources ; clinvar;
Reference 1943692
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ASS1 00000477 NM_000050.4 0000003416 +/+ - 5/16 c.256C>T p.(Arg86Cys) benign(0.131) missense_variant - tolerated(0.09)
ASS1 00000478 NM_054012.3 0000003416 +/+ - 5/16 c.256C>T p.(Arg86Cys) benign(0.131) missense_variant - tolerated(0.09)
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ClinVar @ MSeqDR

RCVaccession RCV000006704; RCV001376621; RCV001555941;
Chromosome 9:133333869..133333869
Allele frequencies from ExAC 0.00004
ClinVar Allele ID 21371
Disease database name and identifier Human Phenotype Ontology:HP:0032397, MONDO:MONDO:0015991, MedGen:C0175683, Orphanet:187|MedGen:C3661900|MONDO:MONDO:0008988, MedGen:C4721769, OMIM:215700, Orphanet:247525
ClinVar preferred disease name Citrullinuria|not provided|Citrullinemia type I
HGVS variant names NC 000009.11:g.133333869C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA253837|OMIM:603470.0012|UniProtKB:P00966#VAR 000683
Gene symbol:Gene id. ASS1:445
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121908644
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None